My specialization is MSN-APRN in Family Nurse Practitioner, Make sure the entire project is centered in one topic only
Instructions
Overview/Description:
My specialization is MSN-APRN in Family Nurse Practitioner, Make sure the entire project is centered in one topic only.
The final project for NSG6101 consists of the development of a novel research proposal specific to your role specialization. The project must include an intervention appropriate to nursing practice and consistent with your MSN role option. An alternative to the above includes the selection of a specialty organization to focus research proposals based on the priorities of that organization. Examples of these organizations could include (but are not limited to): Sigma Theta Tau International, American Nurses’ Foundation, Oncology Nursing Society, Association of Nurses in AIDS Care, American Psychiatric Nursing Association, American Association of Critical Care Nurses, National Association of Pediatric Nurse Associates and Practitioners, National League For Nursing, etc.
Throughout this course you have been developing various sections of the research proposal. This week you will assemble the final proposal (addressing faculty feedback). This paper is to be developed in APA format/style using the required template and not to exceed 8-10 pages (excluding title page/references/appendices).
Criteria:
Introduction
Background and Significance of Problem
Statement of the Problem and Purpose of the Study
Literature Review
Summary of the Evidence for the Proposed Study
Research Question, Hypothesis, and Variables with Operational Definitions
Theoretical Framework
Overview and Guiding Propositions(s) Described in Theory
Application of Theory to Your Study’s/Project’s Focus
Methodology
Sample/Setting: Number and criteria for inclusion and description of place in which data will be collected.
Sampling Strategy
Research Design: Type (e.g., Quasi-Experimental), description, and rationale for selection.
Extraneous Variables (and plan for how controlled).
Instruments: Description, validity, and reliability estimates, which have been performed (on a pre-established measure). Include plans for testing validity and reliability of generating your own instrument(s).
Description of the Intervention
Data Collection Procedures
Data Analysis Plans
Describe plan for data analysis for demographic variables (descriptive statistical tests).
Describe plan for data analysis of study variables (descriptive and inferential statistical tests).
Ethical Issues
Describe ethical considerations and your plan to protect human rights.
Limitation of Proposed Study
Implications for Practice
References
Appendices
Informed Consent Letter
Procedure section is clear, described in detail, specific, and all inclusive. Written in lay language (as documented by reading level score). Includes risks and benefits relevant to study. Address assent (if applicable).
THIS IS WHAT NEEDS TO BE PRIORITIZED ON RUBRIC:
WEEK 3: Variables are operationally defined
WEEK 4: Quality of the initial posting.
WEEK 7: Description of the instrument is appropriate to address research question.
WEEK 8: Data Analysis plan for demographic variables.
Running Head: RESEARCH PROPOSAL METHODOLOGY 1
RESEARCH PROPOSAL METHODOLOGY 2
Research Proposal Methodology
Yulak Landa
Dr. Sandra Allen
May 7, 2020
Methodology
Extraneous variables
I expect a few extraneous variables in my study. First, COVID -19 is not entirely controlled by the use of face masks. Other factors can increase the susceptibility of the participants acquiring the disease. Some of them include the level of hygiene, which is a vague term that you cannot squarely and precisely determine and regulate. Also, the virus is still novel, and there is still very scanty information about it. We do not know everything to do with its gestation, whether it differs across individuals and many other things. Also, we cannot surely guarantee the safety and effectiveness of the test kits and testing reagents being used. We cannot as well determine with precision the availability or lack of any underlying health problem. However, we will follow all the directives given by the Department of Health, such as hand washing techniques, to minimize the exposure in any other way apart from masks. Also, the PPEs will have to have a quality license (Narain, 2020).
Instruments
The study will require personalized protection equipment (PPE), including standard and surgical face masks, gloves, safety shoes and glasses, hard hats, vests, and bodysuits for each of the participants. I would also require the test kits, including the aerosol COVID 19 samples, nasal swabs, throat swabs, and test reagent. We would as well require the disease management equipment like mechanical ventilators plus oxygen supply. All these types of equipment must have been certified for quality to ensure the reliability of the results (Sirinarumitr, 2020).
Intervention
Every participant will need to go through OSHA accepted fit test. There will be no trying to fit in a mask, and participants will have to stick to the provided mask. Instructions will be given t the participants to practice hand hygiene in accordance with CDC guidelines, and trained assistants to the study will be deployed to ensure strict adherence. Some participants may get exposed to the virus and get sick before the testing period. Meaning, the medical personnel will have to be always at the facility to take care of any emergencies and monitor those exposed (Yang, 2019).
Data collection procedures
First, I will visit different care centers to lobby for participation among the caregivers. The participants will be required to undertake necessary tests to ascertain; none of them has a chronic illness or preexisting condition. I will then select randomly taking into account the gender, the participants who will use standard face masks, and those to use surgical masks. The participants will be brought into the laboratory and required to sign the consent form. They will put on all the necessary protective gear, including face masks, before being exposed to a controlled amount of aerosol SARS- COV – 2 viruses. They will then be quarantined for 14 days where before being tested. Any prior showing of any symptom will be tested within the 24-hour bracket. To test nasal swabs will be inserted separately in every participant’s nostrils, and so the throat swap in the pharynx. They will be put under viral transport media, taken to the testing lab. The testing reagents will be used to detect the virus. Those with the disease will be taken to the treatment facility where they will be closely monitored. After seven days, they will be retested to ascertain; they did not acquire the disease (Narain, 2020).
References
Narain, D. S. (2020). Coronavirus outbreak. Journal of Medical Science And clinical Research, 08(04). doi:10.18535/jmscr/v8i4.63
Sirinarumitr, T. (2020). Development of molecular techniques for the detection and pathogenesis study of swine corona-and corona-like virus. Journal of Medicine, 343(2). doi:10.31274/rtd-180813-10812
Yang, T. (2019). A study on control of novel coronavirus (2019-nCoV) disease. Journal of Medical Research, 56, 122. doi:10.37473/fic/10.1101/2020.04.19.20071654
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